Figueroa F, Klein D, Tewarson S, Klein J
J Immunol. 1982 Nov;129(5):2089-93.
Congenic lines B10.KPA42, B10.KPA132, B10.SNA57, B10.DRB62, and B10.WOA105 carry H-2 haplotypes of wild mice on the genetic background of the strain C57BL/10Sn. Two of the lines (B10.DRB62 and B10.WOA105) have H-2 haplotypes indistinguishable from H-2v of B10.SM. The H-2 haplotype of one line (B10.SNA57) seems to have arisen from H-2v by recombination between the D and Qa-2 loci. The H-2 haplotypes of the remaining two lines probably arose from H-2v by recombination between the C4 and D loci. Since all six and no other lines carry the rare Neu-1a allele, the neuraminidase-1 locus is probably located proximal to the H-2D locus. Typing of H-2s recombinants for the enzyme acid phosphatase liver, the processing of which is controlled by the Neu-1 locus, suggests that the locus resides between the E alpha and D loci, that is in the S region.
同源近交系B10.KPA42、B10.KPA132、B10.SNA57、B10.DRB62和B10.WOA105在C57BL/10Sn品系的遗传背景上携带野生小鼠的H-2单倍型。其中两个品系(B10.DRB62和B10.WOA105)的H-2单倍型与B10.SM的H-2v无法区分。一个品系(B10.SNA57)的H-2单倍型似乎是由H-2v通过D和Qa-2位点之间的重组产生的。其余两个品系的H-2单倍型可能是由H-2v通过C4和D位点之间的重组产生的。由于所有这六个品系而没有其他品系携带罕见的Neu-1a等位基因,神经氨酸酶-1位点可能位于H-2D位点的近端。对肝脏酸性磷酸酶(其加工由Neu-1位点控制)的H-2s重组体进行分型表明,该位点位于Eα和D位点之间,即在S区域。